Download Caenorhabditis elegans: Molecular Genetics and Development by John H. Rothman, Andrew Singson PDF
By John H. Rothman, Andrew Singson
An up to date variation of the classic Methods in telephone Biology quantity forty eight, this book emphasizes various tools and applied sciences had to examine C. elegans, either as an built-in organism and as a version procedure for examine inquiries in cellphone, developmental, and molecular biology, in addition to in genetics and pharmacology. via directing its audience to tried-and-true and state-of-the-art recipes for research, this finished assortment is meant to lead investigators of C. elegans for years yet to come. *Diverse, updated innovations covered will be worthy to the broadening group of C. elegans researchers for future years* Chapters written through leaders within the box* attempted and actual tools bring busy researchers a one-stop compendium of crucial protocols
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Additional info for Caenorhabditis elegans: Molecular Genetics and Development
Although crossing over can occur in the inverted region, recombination between the breakpoints is almost completely suppressed in heterozygotes due to topological restraints, absence of DNA alignment, or disruption of sites required for pairing. When recombination 35 2. Specialized Chromosomes and Their Uses in Caenorhabditis elegans Table III A listing of genomic balancers that are available for use in C. , 1993) chromosome sC1 (III) [D. Baillie, LG III from unc-45 to pers. ] $daf-2 sC4 (V) [D.
And Waterston, R. H. (1986). Molecular cloning of the muscle gene unc22 in Caenorhabditis elegans by Tc1 transposon tagging. Proc. Natl Acad. Sci. A. 83, 2579–2583. , and Conradt, B. (2010). Transcriptional upregulation of both egl-1 BH3-only and ced-3 caspase is required for the death of the male-specific CEM neurons. Cell Death Differ. 17, 1266–1276. 22 Eric J. Lambie Rogalski, T. , Moerman, D. , and Baillie, D. L. (1982). Essential genes and deficiencies in the unc-22 IV region of Caenorhabditis elegans.
Translocations are often marked with a mutation, which results in a phenotype that makes the homozygote readily observable (‘‘Visible’’), thus facilitating selection of the heterozygote. In this way, either lethal or visible mutants can be balanced and the strain can be maintained in a heritably stable manner. The reciprocal translocation, eT1, illustrates the properties and uses of translocations in C. elegans. eT1, originally thought to be a mutation in an unc gene, was shown to have exchanged the right portion of chromosome III for the left portion of chromosome V without the loss of any essential material, and thus is homozygous viable (Rosenbluth and Baillie, 1981).